FDA 510(k) Application Details - K220473

Device Classification Name	Indicator, Biological Sterilization Process   More FDA Info for this Device
510(K) Number	K220473
Device Name	Indicator, Biological Sterilization Process
Applicant	STERIS 5960 Heisley Rd. Mentor, OH 44060 US Other 510(k) Applications for this Company
Contact	Anthony Piotrkowski Other 510(k) Applications for this Contact
Regulation Number	880.2800   More FDA Info for this Regulation Number
Classification Product Code	FRC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/18/2022
Decision Date	03/18/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review